Candidate genes and biological processes in de novo CNVs from autistic individuals

Samankaltaisia teoksia

• 46% of individuals with ASD that harbour de novo CNVs have at least one de novo CNV that overlaps a gene associated with synaptic signalling
  Tekijä: Webber, C, et al.
  Julkaistu: (2010)
• Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
  Tekijä: Webber, C, et al.
  Julkaistu: (2009)
• Accurate distinction of pathogenic from benign CNVs in mental retardation.
  Tekijä: Hehir-Kwa, J, et al.
  Julkaistu: (2010)
• Synergistic interactions between Drosophila orthologues of genes spanned by de novo human CNVs support multiple-hit models of autism.
  Tekijä: Stuart J Grice, et al.
  Julkaistu: (2015-03-01)
• Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
  Tekijä: Caleb Webber, et al.
  Julkaistu: (2009-06-01)